Production Technician (Fixed-Term)

Novartis Italia; Saluggia; In loco; EUR 30.000 - 40.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Saluggia is seeking a Production Technician for aseptic manufacturing within the Sterile Area. The ideal candidate will have a scientific technical degree and experience in a regulated environment. Responsibilities include controlling raw materials, preparing solutions, and ensuring compliance with GMP requirements. Fluency in Italian and attention to detail are essential. Join us to make a difference in patients' lives.

Servizi

Career growth opportunities

Comprehensive benefits

Collaborative work environment

Competenze

• Previous experience in a similar role within a highly regulated environment (ideally GMP).
• Basic knowledge of English.

Mansioni

• Responsible for the control of Raw Materials for the manufacturing of the sterile batch.
• Prepare product bulk solutions and set up the machine for filling, stoppering, and crimping vials.
• Participate in the Media Fill execution.
• Observe behavioral standards and flow of materials in controlled contamination areas.
• Sterilize and de-aerate glassware and caps as per internal procedures.
• Perform visual inspection manually and using the semi-automatic screamer machine.
• Document activities performed during the manufacturing process.
• Support maintenance department during maintenance activities.
• Act as referent of the aseptic process for production line improvements.

Conoscenze

Fluent in Italian

Detail oriented

Formazione

Scientific technical degree

Descrizione del lavoro

Summary

The Production Technician works in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation.

About The Role

Major accountabilities

• Responsible for the control of Raw Materials (MP) for the manufacturing of the sterile batch (e.g. labels, shelf‑life, compliance with BR).
• Prepare in the Sterile Area product bulk solutions and set up the machine for filling, stoppering and crimping vials, execute production activities in Sterile Area, according to the Batch Record instructions aseptic behavior instructions and SOPs, label and package the products.
• Participate in the Media Fill execution.
• Observe behavioral standards and flow of materials in the areas with controlled contamination (and with regard to the sterile room) in compliance with the internal procedures.
• Sterilize in an autoclave and dry caps and capsules in the oven according to the internal procedures; de‑aerate flasks and glassware in the oven to be used in the subsequent processing phases.
• Perform cleaning and washing of the glassware and bottles to be used in the subsequent processing steps in accordance with the procedures laid down by the specific procedures.
• Perform visual inspection, manually and using the semi‑automatic screamer machine.
• Keep track in a timely manner of all the activities performed during the manufacturing process, as per Data Integrity, SOPs instruction and GMP requirements.
• Support maintenance department during ordinary and extraordinary maintenance activities.
• Referent of aseptic process for the improvement of the production lines.

Essential Requirements

• Scientific technical degree.
• Previous experience in a similar role within a highly regulated environment (ideally GMP).
• Fluent in Italian. Basic knowledge of English.
• Detail oriented.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

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Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards